Carprieve Tablets 20 mg
Carprofen
Last verified
Veterinary medicinal product: tablet. Distribution category: POM-V (Veterinary Medicines Regulations 2013, Schedule 3). Active substance: Carprofen.1
In short: questions and answers
- Does Carprieve Tablets 20 mg need a prescription?
- Prescription only. As stated in the registration decision.1
- Which animals is Carprieve Tablets 20 mg for?
- Dogs.1
- What is the active substance in Carprieve Tablets 20 mg?
- Carprofen. ATCvet code: QM01AE91.13
- What is the withdrawal period of Carprieve Tablets 20 mg according to the leaflet?
- No withdrawal period is set for this drug: it is not intended for food-producing animals.3
- Dispensing
- Prescription only1
POM-V: Prescription Only Medicine - Veterinarian. Supplied only on a prescription written by a veterinary surgeon who has assessed the animal.12
Supplied only on a veterinarian's prescription. As stated in the registration decision.
- Animal species
- Dogs1
- Active substance
- Carprofen
- ATCvet code
- QM01AE913
- Manufacturer
- Marketing authorisation holder: Norbrook Laboratories Limited
Withdrawal period
No withdrawal period is set for this drug: it is not intended for food-producing animals.3
Summary of product characteristics
Composition
Active Substance:
Each tablet contains:
Carprofen 20 mg
Excipients:
For a full list of excipients, see section 6.1
6.1 List of excipients
Microcrystalline cellulose
Lactose monohydrate
Croscarmellose sodium
Poly-vinyl pyrrolidone K 30
Sodium laurilsulfate
Magnesium stearate
Purified water
Pharmaceutical form
Tablet
A white/off white circular tablet of diameter 8 mm, 20 embossed on one side and a single break line on the other side.
Pharmacological properties
Pharmacotherapeutic group: Non-steroidal anti-inflammatory drug
ATC Vet Code: QM01AE91
5.1 Pharmacodynamic properties
Carprofen, (±)-6-chloro-α-methylcarbazole-2-acetic acid, is a non-steroidal anti- inflammatory drug (NSAID). It is a derivative of phenylpropionic acid and a member of the arylpropionic acid class of NSAIDs. As a representative of the 2-arylpropionic family, it contains a chiral center at C2 of the propionic moiety and therefore, exists in 2 sterioisomeric forms, the (+)-S and (-)-R enantiomers.
5.2 Pharmacokinetic properties
Following oral administration of 4mg carprofen/kg to dogs, peak plasma concentrations (mean Cmax = 28.51 µg/ml) were achieved in 4 hours.
Absorption of carprofen is rapid and complete in the dog. The volume of distribution is small with the highest drug concentrations occurring in plasma. Ratios of tissue to plasma concentration are less than one, which is consistent with a high level of binding of carprofen to plasma proteins.
Target species
Dogs
Indications
For analgesia and reduction of chronic inflammation, for example in degenerative joint disease, in dogs.
Carprieve Tablets can also be used in the management of post-operative pain.
Dosage
For oral administration.
An initial dose of 2 to 4 mg carprofen/kg bodyweight/day is recommended to be given in 2 equally divided doses. The dose may be reduced to 2 mg carprofen/kg bodyweight/day administered as a single daily dose after 7 days, subject to clinical response.
Duration of treatment will be dependent upon the response seen. Long term treatment should be under regular veterinary supervision.
To extend analgesic cover post-operatively, parenteral administration of carprofen, may be followed with Carprieve Tablets.
Contraindications
The use of Carprieve Tablets is contraindicated in the cat, and the inadvertent administration of oral carprofen tablets may induce life-threatening conditions in this species.
Do not exceed the stated dose.
Do not administer NSAIDs concurrently or within 24 hours of each other. Some NSAIDs may be highly bound to plasma proteins and compete with other highly bound drugs, which can lead to toxic effects.
Do not use in dogs suffering from cardiac, hepatic or renal disease, where there is a possibility of gastrointestinal ulceration or bleeding, or where there is evidence of a blood dyscrasia or hypersensitivity to the product.
In the absence of any specific studies in pregnant bitches such use is not indicated.
Adverse reactions
None.
Warnings
Special precautions for use in animals
None.
Special precautions to be taken by the person administering the veterinary medicinal product to animals
None.
Use during pregnancy, lactation or lay
In the absence of any specific studies in pregnant bitches such use is not indicated.
Interactions
Do not administer NSAIDs concurrently or within 24 hours of each other. Some NSAIDs may be highly bound to plasma proteins and compete with other highly bound drugs, which can lead to toxic effects.
Concurrent administration of potential nephrotoxic drugs should be avoided.
Overdose
Not applicable.
Special warnings
Use in dogs less than 6 weeks of age, or in aged animals, may involve additional risk. If such use cannot be avoided, such dogs may require a reduced dosage and careful clinical management.
Avoid use in any dehydrated, hypovolaemic or hypotensive dog, as there is a potential risk of increased renal toxicity.
NSAIDs can cause inhibition of phagocytosis and hence in the treatment of inflammatory conditions associated with bacterial infection, appropriate concurrent antimicrobial therapy should be instigated.
Withdrawal period
Not applicable
Incompatibilities
None.
Immediate packaging
Carprieve Tablets are supplied in:
Polypropylene Snap Secure Tubs, containing 100 tablets, sealed with a white Polyethylene Snap Secure Cap.
Alu/Alu blister strips of 2 x 5 tablets
Storage
Do not store above 25ºC.
Store in a dry place.
Protect from light.
Shelf life
Tubs: 36 months
Blister strips: 24 months
Disposal of unused product
Any unused product or waste material should be disposed of in accordance with national requirements.
Additional information
ManA: 2000 Vm: 02000/4220
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
5th September 2003/ 5th September 2008
10 DATE OF REVISION OF THE TEXT
January 2009
Registration holder
Norbrook Laboratories Limited
Station Works
Newry
Co. Down, BT35 6JP
Northern Ireland
Regulations
- Veterinary Medicines Regulations 2013 (SI 2013/2033), Schedule 32
Sources
- VMD Product Information Database: Carprieve Tablets 20 mg, 02000/4220
- The Veterinary Medicines Regulations 2013, Schedule 3 (categories of veterinary medicinal products)
- Summary of Product Characteristics: Carprieve Tablets 20 mg
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